Webinar Premiere

Big Benefits, Scalable Price: The SAS® Cloud-Based Clinical Platform for SMBs

Learn how small-to-midsize pharmas, biotechs, medical device manufacturers and CROs can benefit from a compliant cloud-based solution to facilitate clinical trials.

March 10 • 10 a.m. ET • Cost: Complimentary

About the webinar

Collecting, managing, standardizing and analyzing clinical trial data is crucial in the clinical submission process for regulatory approval for new medical or biotech devices.

SAS has a scalable solution to help small-to-midsize organizations with the clinical trial process.

We’ll demo the SAS Life Science Analytics Framework and show how it can benefit small-to-midsize organizations (pharma, biotech, medical device and CRO).

What you'll learn:

  • How the SAS framework can help define and manage policies to ensure FDA compliance.
  • How to easily drive collaboration and workflow between preclinical, biostatistics, operations and medical affairs.
  • How you can end the struggle with the management and implementation of clinical data standards (CDASH, SDTM, SEND, ADaM and Define-XML).
  • How you can quickly answer regulatory inquiries and trace data pedigree back to the source.

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About the Experts

Speaker 1

Molly Jones
Senior Pre-Sales Solutions Architect, SAS

Speaker 2

Elena Wojciechowski
Senior Associate Inside Sales Account Executive, SAS

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